HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Methyl 2-propen-1-yl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Product | Carbonic acid, di-2-propen-1-yl ester | HCID 84764 | 2% |
| Product | Methyl 2-propen-1-yl carbonate | HCID 534788 | 23.8% |
Reaction Steps
The procedure employed in Example 30 is substantially repeated employing polystyrene-bound benzyl-tri-n-butylphosphonium chloride (2 percent cross-linked with divinylbenzene) as the catalyst. Accordingly, 15 g of the polymeric catalyst, allyl chloride (76.5 g, 1.0 mole), dimethyl carbonate (90.0 g, 1.0 mole) and p-methoxyphenol (0.5 g, 0.004 mole) are combined in a reactor and heated for 6 hours at 150° C. under 600 psi carbon dioxide. The reactor is then cooled to room temperature and vented. After separating the catalyst by filtration, allyl methyl carbonate (23.8 percent yield) and diallyl carbonate (2.0 percent yield) are obtained by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04658041 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-4f3bbf06cf34442bb82258a844796983 |
| Source note | uspto-grants-1987_04 |